{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80755",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states:  AL, AR, AZ, CA, CO, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WY, and Puerto Rico.    The products were distributed to the following foreign countries: Chile, Ecuador, Japan, Netherlands.",
      "recall_number": "Z-3132-2018",
      "product_description": "Affixus¿ Hip Fracture Nail 130¿ 13 mm x 180 mm, Item Number: 814513180",
      "product_quantity": "5947 total",
      "reason_for_recall": "The set screw is not able to advance or reverse from the original position in the nail.",
      "recall_initiation_date": "20180717",
      "center_classification_date": "20180913",
      "termination_date": "20200602",
      "report_date": "20180919",
      "code_info": "063590  063600  220020  245510  290720  371210  482750  482760  482770  523410  097180  188350  188370  290690  970510  970530  970580"
    }
  ]
}